Cas 439114-60-0,<i>N</i>-{9-[5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-3-yl]-9<i>H</i>-purin-6-yl}-benzamide

439114-60-0

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Basic information

Product Name: N-{9-[5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-3-yl]-9H-purin-6-yl}-benzamide
Synonyms:
CAS NO:439114-60-0
Molecular Formula:
Molecular Weight: 449.509
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-{9-[5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-3-yl]-9H-purin-6-yl}-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{9-[5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-3-yl]-9H-purin-6-yl}-benzamide(439114-60-0)
EPA Substance Registry System: N-{9-[5-(1,4-dioxa-spiro[4.5]dec-2-yl)-tetrahydro-furan-3-yl]-9H-purin-6-yl}-benzamide(439114-60-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 439114-60-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 439114-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,1,1 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 439114-60:
(8*4)+(7*3)+(6*9)+(5*1)+(4*1)+(3*4)+(2*6)+(1*0)=140
140 % 10 = 0
So 439114-60-0 is a valid CAS Registry Number.

439114-60-0Upstream product

439114-55-3 (2S,4R)-4-(p-tolylsulfonyloxy)-2-[(1R)-1,2-cyclohexylidenedioxyethyl]tetrahydrofuran

439114-60-0Downstream Products

439114-58-6 9-{(3S,5S)-5-[(1R)-1,2-dihydroxyethyl]tetrahydrofuran-3-yl}-N⁶-benzoyladenine

439114-60-0Relevant academic research and scientific papers

A facile and simple entry into isodideoxynucleosides

Chattopadhyay, Angshuman,Salaskar, Avinash

, p. 785 - 789 (2002)

Sharpless asymmetric dihydroxylations of homoallylic alcohol derivative 3 with AD mix-α afforded α addition product 4a predominantly. Compound 4a was produced with very high selectivity when 3 was treated with AD mix-β. The inherent hydroxylic functionali

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